Evidence map›Paper›PMID 35703369›Full record

ArticleMedical physics2022

Accelerated cardiac T1 mapping with recurrent networks and cyclic, model-based loss.

Johnathan V Le, Jason K Mendes, Nicholas McKibben, Brent D Wilson, Mark Ibrahim, Edward V R DiBella, Ganesh Adluru

Open access · greenAbstract read
In one paragraph

Article in Medical physics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.4field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 18 citations in OpenAlex.

  1. Respiratory navigator-guided multi-slice free-breathing cardiac TPhysics and imaging in radiation oncology · 2025
    Article
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  6. Scanner-Independent MyoMapNet for Accelerated Cardiac MRI TJournal of magnetic resonance imaging : JMRI · 2024
    Article
  7. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Johnathan V LeUtah Center for Advanced Imaging Research (UCAIR), Department of Radiology and Imaging Sciences, University of Utah, Salt Lake City, Utah, USA.
Jason K MendesUtah Center for Advanced Imaging Research (UCAIR), Department of Radiology and Imaging Sciences, University of Utah, Salt Lake City, Utah, USA.
Nicholas McKibbenUtah Center for Advanced Imaging Research (UCAIR), Department of Radiology and Imaging Sciences, University of Utah, Salt Lake City, Utah, USA.
Brent D WilsonDivision of Cardiovascular Medicine, University of Utah, Salt Lake City, Utah, USA.
Mark IbrahimDivision of Cardiovascular Medicine, University of Utah, Salt Lake City, Utah, USA.
Edward V R DiBellaUtah Center for Advanced Imaging Research (UCAIR), Department of Radiology and Imaging Sciences, University of Utah, Salt Lake City, Utah, USA.
Ganesh AdluruUtah Center for Advanced Imaging Research (UCAIR), Department of Radiology and Imaging Sciences, University of Utah, Salt Lake City, Utah, USA.
University of Utah · USAdvanced Imaging Research (United States) · US

Funding

Improved Estimation of Ischemic Burden with Cardiac MRIR01HL138082 · NHLBI · UNIVERSITY OF UTAH · PI ADLURU, GANESH · 2017 to 2020
$1.5M
Siemens MAGNETOM Prisma 3T MRI scannerS10OD018482 · OD · UNIVERSITY OF UTAH · PI PARKER, DENNIS L · 2015 to 2015
$1.2M
NHLBI NIH HHS R01 HL138082NIH HHS S10 OD018482
6 · The paper itself

Abstract

backgroundUsing the spin-lattice relaxation time (T1) as a biomarker, the myocardium can be quantitatively characterized using cardiac T1 mapping. The modified Look-Locker inversion (MOLLI) recovery sequences have become the standard clinical method for cardiac T1 mapping. However, the MOLLI sequences require an 11-heartbeat breath-hold that can be difficult for subjects, particularly during exercise or pharmacologically induced stress. Although shorter cardiac T1 mapping sequences have been proposed, these methods suffer from reduced precision. As such, there is an unmet need for accelerated cardiac T1 mapping. PURPOSE: To accelerate cardiac T1 mapping MOLLI sequences by using neural networks to estimate T1 maps using a reduced number of T1-weighted images and their corresponding inversion times. MATERIALS AND

methodsIn this retrospective study, 911 pre-contrast T1 mapping datasets from 202 subjects (128 males, 56 ± 15 years; 74 females, 54 ± 17 years) and 574 T1 mapping post-contrast datasets from 193 subjects (122 males, 57 ± 15 years; 71 females, 54 ± 17 years) were acquired using the MOLLI-5(3)3 sequence and the MOLLI-4(1)3(1)2 sequence, respectively. All acquisition protocols used similar scan parameters:

resultsOur proposed network demonstrated similar T1 estimations to the standard MOLLI sequences (pre-contrast:

conclusionsA bidirectional multilayered LSTM network with fully connected output and cyclic model-based loss was used to generate high-quality pre- and post-contrast T1 maps using the first three T1-weighted images and their corresponding inversion times. This work demonstrates that combining deep learning with cardiac T1 mapping can potentially accelerate standard MOLLI sequences from 11 to 3 heartbeats.

Indexed as

HeartMagnetic Resonance ImagingFemaleGadoliniumHeterocyclic CompoundsHumansMaleMyocardiumOrganometallic CompoundsPhantoms, ImagingReproducibility of ResultsRetrospective StudiesGadoliniumgadoteridolHeterocyclic CompoundsOrganometallic Compoundscardiacdeep learningMRIquantitative imagingT1 mapping

Identifiers

PMID35703369
PMCPMC9742165
OpenAlexW4282922307

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.